Canonical Allele Identifier: CA493799392

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16263573A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169716A>G , CM000678.2:g.16169716A>G	GRCh38
NC_000016.9:g.16263573A>G , CM000678.1:g.16263573A>G	GRCh37
NC_000016.8:g.16171074A>G	NCBI36
NG_007558.2:g.58756T>C
NG_007558.3:g.58902T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2925T>C	ENSP00000483331.2:p.Pro975=
ENST00000205557.12:c.2925T>C MANE Select	ENSP00000205557.7:p.Pro975=
ENST00000205557.11:c.2925T>C	ENSP00000205557.7:p.Pro975=
ENST00000456970.6:c.2750T>C	ENSP00000405002.2:n.2750T>C
ENST00000622290.4:c.*134T>C	ENSP00000483331.1:n.*134T>C
NM_001171.5:c.2925T>C	NP_001162.4:p.Pro975=
XM_011522479.1:c.2892T>C	XP_011520781.1:p.Pro964=
XM_011522480.1:c.2583T>C	XP_011520782.1:p.Pro861=
XM_011522481.1:c.2583T>C	XP_011520783.1:p.Pro861=
XR_932836.1:n.3160T>C
XR_932837.1:n.3161T>C
XR_932838.1:n.3161T>C
NM_001351800.1:c.2583T>C	NP_001338729.1:p.Pro861=
NR_147784.1:n.2787T>C
XM_011522479.2:c.2892T>C	XP_011520781.1:p.Pro964=
XM_011522481.3:c.2583T>C	XP_011520783.1:p.Pro861=
XM_017023212.1:c.2757T>C	XP_016878701.1:p.Pro919=
XM_017023214.1:c.2925T>C	XP_016878703.1:p.Pro975=
XM_024450261.1:c.2961T>C	XP_024306029.1:p.Pro987=
XR_932836.2:n.3106T>C
XR_932837.3:n.3106T>C
XR_932838.3:n.3106T>C
NM_001171.6:c.2925T>C MANE Select	NP_001162.5:p.Pro975=